6-(Benzyloxy)-9-((1S,3R,3S)-4-(benzyloxy)-3-(benzyloxymethyl)-2-methylenecyclopentyl)-N-((4-methoxyphenyl)diphenylmethyl)-9H-purin-2-amine

97%

Reagent Code: #50267
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CAS Number 142217-80-9

science Other reagents with same CAS 142217-80-9

blur_circular Chemical Specifications

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Weight 819.99 g/mol
Formula C₅₃H₄₉N₅O₄
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of complex nucleoside analogs, which are critical in the development of antiviral and anticancer drugs. Its structure is particularly valuable for designing molecules that can inhibit viral replication or target specific cancer cells. Researchers often employ it in the preparation of prodrugs, where its protective groups can be selectively removed to release the active drug at the desired site. Additionally, its unique stereochemistry and functional groups make it a valuable tool in studying enzyme interactions and drug delivery mechanisms. Its application extends to the development of nucleotide-based therapies, where it aids in enhancing the stability and bioavailability of therapeutic agents.

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inventory 100mg
10-20 days ฿1,062.00

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6-(Benzyloxy)-9-((1S,3R,3S)-4-(benzyloxy)-3-(benzyloxymethyl)-2-methylenecyclopentyl)-N-((4-methoxyphenyl)diphenylmethyl)-9H-purin-2-amine
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of complex nucleoside analogs, which are critical in the development of antiviral and anticancer drugs. Its structure is particularly valuable for designing molecules that can inhibit viral replication or target specific cancer cells. Researchers often employ it in the preparation of prodrugs, where its protective groups can be selectively removed to releas

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of complex nucleoside analogs, which are critical in the development of antiviral and anticancer drugs. Its structure is particularly valuable for designing molecules that can inhibit viral replication or target specific cancer cells. Researchers often employ it in the preparation of prodrugs, where its protective groups can be selectively removed to release the active drug at the desired site. Additionally, its unique stereochemistry and functional groups make it a valuable tool in studying enzyme interactions and drug delivery mechanisms. Its application extends to the development of nucleotide-based therapies, where it aids in enhancing the stability and bioavailability of therapeutic agents.

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